Stabilization of 1,1,1-trichloroethane



United States Patent US. Cl. 260-652.5 5 Claims ABSTRACT OF THE DISCLOSURE The reaction of 1,1,l-trichloroethane with aluminum is inhibited by the presence in the 1,1,l-trichloroethane of a small amount of a dissolved nitrobenzaldehyde compound. Concentrations of the order of 001-1 gram mole per liter provide significant inhibition.

Background of the invention This invention relates to the stabilization of chlorinatecl solvents. More particularly, the present invention concerns the stabilization of l,l,l-trichloroethane in the presence of metallic aluminum.

Chlorinated hydrocarbons such as trichloroethylene and perchloroethylene are commonly used as solvents in chemical processes, dry cleaning, and metal degreasing. Solvents of this type are subject to slow decomposition and oxidation reactions, particularly in the presence of impurities such as water, traces of acid or metal salts. Corrosion of metal surfaces in containers and process equipment and deterioration of solvent quality by formation of acidic and colored byproducts thereby become serious problems. Inhibitors such as acid scavengers and antioxidants are commonly added to these solvents in order to prevent such degradative reactions. Inhibitor concentrations are noramlly of the order of one percent by weight or less.

1,1,1-trichloroethane poses a particularly difficult stabilization problem because of its unusual reactivity with certain metals, notably aluminum. Traces of metal salts, moisture, or other impurities are not needed to initiate the 1,1,1-trichloroethane-aluminum reaction, for this reaction occurs spontaneously on a freshly exposed aluminum surface with spectacular results, converting the solvent and the metal surface in a few minutes to a blackened mass of acidic, carbonaceous material and aluminum salts. Conventional acid acceptor stabilizers cannot be depended upon to inhibit the aluminum-l,1,1-trichloroethane reaction and suitable inhibitors must be discovered by independent investigation. The search has yielded few effective compounds and these show little or no obvious pattern of structure. Typical 1,1,l-trichloroethane formulations contain about five percent by weight of inhibitor which is usually a combination of compounds to inhibit reaction of the solvent with a variety of metals.

Summary of the invention It has now been found that the 1,1,1-trichloroethanealuminum reaction can be substantially retarded or prevented by incorporating into the 1,1,l-trichloroethane an inhibiting amount of a nitrobenzaldehyde compound of the formula CHO "ice

wherein R is hydrogen or lower alkyl of l-4 carbon atoms. Such compounds may be used alone or in any combination with each other or with other non-reactive conventional inhibitors.

Detailed description Only a quantity of nitrobenzaldehyde compound sufficient to retard or to stop the reaction of aluminum and 1,1,l-trichloroethane need be used. Although any significant amount will provide some inhibition, preferably about 0.0l1 gram mole per liter of 1,1,1-trichloroethane is employed and about 0.03-01 gram mol is usually most preferred.

Nitrobenzaldehyde compounds as defined by the general formula set forth above were tested for inhibiting activity in elongated glass test tubes having an inside diameter of 0.8 cm. and 33 cm. in length. To each vertically disposed tube there was added 0.54 g. of essentially pure l632 mesh granular aluminum and a solution of the inhibitor in purified 1,1,l-trichloroethane to make a total volume of test mixture of 5 ml. The closed ends of the test tubes were then immersed in an oil bath held at a temperature sufiicient to maintain the 1,1,1-trichloroethane solution in each tube at a steady reflux. The results listed in the following examples indicate the minimum concentration of the inhibitor found effective to provide complete inhibtion of the 1,1,l-trichloroethane-aluminum reaction for 24 hours under these conditions. Prevention of the reaction for this length of time under the described conditions indicates capacity for effective inhibition for an indefinite period. Concentrations are given in gram moles per liter, this figure being convertible to weight percent by the equation (moles/liter) (mol. Wt. of inhibitor) wt. percent 1346 For example, a concentration of 0.10 g. mole per liter of an inhibitor of molecular weight 134.6 is equal to 1.0 weight percent of that inhibitor.

Efiective concentra- Examplo Compound name tion, g. moles/liter 1 o-Nitrobenzaldehyde 0. 1

2 m-Nitrobenzaldehyde 0.05 3 p-Nitrobenzaldehyde 0.04

wherein R is hydrogen or lower alkyl.

2. The composition of claim 1 wherein the concentration of the nitrobenzaldehyde compound is 0.01-1 g. mole per liter.

3. The composition of claim 1 wherein R is hydrogen.

4. The composition of claim 3 wherein the nitrobenzaldehyde compound is m-nitrobenzaldehyde.

5. The composition of claim 3 wherein the nitrobenzaldehyde compound is p-nitrobenzaldehyde.

4 References Cited Continental Oil, Chemi. Abst., vol. 64, col. 4746A (1966). LEON ZITVER, Primary Examiner. MATTHEW M. JACOB, Assistant Examiner.

US. Cl. X.R. 252171 

